Synthesis of via a tandem sharpless asymmetric dihydroxylation/lipase-catalyzed transesterification
1995; Elsevier BV; Volume: 36; Issue: 24 Linguagem: Inglês
10.1016/0040-4039(95)00778-b
ISSN1873-3581
AutoresAditya Sobti, Gary A. Sulikowski,
Tópico(s)Enzyme Catalysis and Immobilization
ResumoAn enantioselective synthesis of the trideoxy sugar 4-O-acetyl-l-rhodinopyranose (7) is described. A key feature of the synthetic strategy is a Sharpless asymmetric dihydroxylation followed by a lipase-mediated mono-esterification of the resultant diol (3→4→6).
Referência(s)